rs3819294
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs3819294(C;T) |
Make rs3819294(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31354710 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs3819294 |
dbSNP (classic) | rs3819294 |
ClinGen | rs3819294 |
ebi | rs3819294 |
HLI | rs3819294 |
Exac | rs3819294 |
Gnomad | rs3819294 |
Varsome | rs3819294 |
LitVar | rs3819294 |
Map | rs3819294 |
PheGenI | rs3819294 |
Biobank | rs3819294 |
1000 genomes | rs3819294 |
hgdp | rs3819294 |
ensembl | rs3819294 |
geneview | rs3819294 |
scholar | rs3819294 |
rs3819294 | |
pharmgkb | rs3819294 |
gwascentral | rs3819294 |
openSNP | rs3819294 |
23andMe | rs3819294 |
SNPshot | rs3819294 |
SNPdbe | rs3819294 |
MSV3d | rs3819294 |
GWAS Ctlg | rs3819294 |
GMAF | 0.1276 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs3819294(T;T) |
Alt | rs3819294(T;T) |
Reference | Rs3819294(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31322487G>A |
CLNSRC | |
CLNACC |